(Q128381)

HARMINE (English)

19 October 2016

C₁₃H₁₂N₂O

1 reference

HARMINE (English)

19 November 2016

CC1=NC=CC2=C1NC3=C2C=CC(=C3)OC

1 reference

HARMINE (English)

19 November 2016

264 degree Celsius

1 reference

Jean-Claude Bradley Open Melting Point Dataset

found in taxon

Peganum harmala

22 references

Chemical and biological investigation of harmal plant. 2. Alkaloidal investigation

Isoharmine, a β-carboline alkaloid from Peganum harmala seeds

New alkaloids from Peganum harmala

Antibacterial and antifungal activities of (beta)-carboline alkaloids of Peganum harmala (L) seeds and their combination effects.

Trace analysis of harman alkaloids in passiflora incarnata by reversed-phase high performance liquid chromatography

Deoxypeganidine — A new alkaloid from Peganum harmala

Pegamine: A new alkaloid fromPeganum harmala

Method for the quantitative determination of deoxypeganine from Peganum harmala

Polybuffer separation of the combined alkaloids of Peganum harmala

The dynamics of the accumulation of alkaloids in Peganum harmala

Lipids from the aerial part of Peganum harmala

Biosynthesis of serotonin and β-carboline alkaloids in hairy root cultures of Peganum harmala

Harmalidine, A β-carboline alkaloid from peganum harmala

An oxamide from Peganum harmala seeds

Antimicrobial Agents From Higher Plants. Antimicrobial Agents From Peganum harmala Seeds

The biogenesis of certain alkaloids

Production of β-Carboline Alkaloids in Transformed Root Cultures of Peganum harmala L.

Hairy Root Cultures of Peganum harmala II. Characterization of Cell Lines and Effect of Culture Conditions on the Accumulation of ß-Carboline Alkaloids and Serotonin

Alkaloidal constituents ofpeganum harmala and synthesis of the minor alkaloid deoxyvascinone

Alkaloids ofPeganum harmala

Synthesis of quaternary salts of Peganum harmala alkaloids

Alkaloids and phenylpropanoids from Peganum nigellastrum

Peganum nigellastrum

3 references

Triterpenoids from Peganum nigellastrum

Alkaloids and phenylpropanoids from Peganum nigellastrum

Alkaloids derived from genus Veratrum and Peganum of Mongolian origin as multidrug resistance inhibitors of cancer cells

Cashew

1 reference

Quantitative analysis of all types of β-carboline alkaloids in medicinal plants and dried edible plants by high performance liquid chromatography with selective fluorometric detection

Passiflora incarnata

5 references

Quantitative analysis of all types of β-carboline alkaloids in medicinal plants and dried edible plants by high performance liquid chromatography with selective fluorometric detection

Trace analysis of harman alkaloids in passiflora incarnata by reversed-phase high performance liquid chromatography

High-Speed Extraction and HPLC Fingerprinting of Medicinal Plants – II. Application to Harman Alkaloids of Genus Passiflora

IDENTIFICATION AND SIMULTANEOUS ANALYSIS OF HARMANE, HARMINE, HARMOL, ISOVITEXIN, AND VITEXIN INPASSIFLORA INCARNATAEXTRACTS WITH A NOVEL HPLC METHOD

Studies on passiflora incarnata dry extract. I. Isolation of maltol and pharmacological action of maltol and ethyl maltol

Pinellia ternata

1 reference

Quantitative analysis of all types of β-carboline alkaloids in medicinal plants and dried edible plants by high performance liquid chromatography with selective fluorometric detection

Simira williamsii

1 reference

Inhibiting Activity of Some Glucoindolalkaloids and Iridoids fromSickingia williamsiion Electrically Induced Contractions of Isolated Guinea-pig Ileum

Acraea andromacha

1 reference

High-performance liquid chromatographic identification of simple β-carboline alkaloids in specimens of heliconiini butterflies

Banisteriopsis caapi

3 references

Monoamine oxidase inhibitors in South American hallucinogenic plants: tryptamine and beta-carboline constituents of ayahuasca

Banisteriopsis caapi, a unique combination of MAO inhibitory and antioxidative constituents for the activities relevant to neurodegenerative disorders and Parkinson's disease

The alkaloid of Banisteriopsis inebrians Morton

Festuca pratensis

1 reference

Paper chromatography of alkaloids of tall fescue hay

Grewia bicolor

1 reference

Investigation of Grewia bicolor Juss

Kopsia griffithii

1 reference

Leishmanicidal alkaloids from Kopsia griffithii

Oxalis tuberosa

1 reference

Exudation of fluorescent beta-carbolines from Oxalis tuberosa L roots

Oxytropis puberula

2 references

Alkaloids of Oxytropis puberula

Muricatisine — A new alkaloid from two species ofOxytropis

Passiflora actinia

1 reference

High-Speed Extraction and HPLC Fingerprinting of Medicinal Plants – II. Application to Harman Alkaloids of Genus Passiflora

Passiflora alata

1 reference

High-Speed Extraction and HPLC Fingerprinting of Medicinal Plants – II. Application to Harman Alkaloids of Genus Passiflora

Passiflora auriculata

1 reference

High-Speed Extraction and HPLC Fingerprinting of Medicinal Plants – II. Application to Harman Alkaloids of Genus Passiflora

Passiflora boenderi

1 reference

High-Speed Extraction and HPLC Fingerprinting of Medicinal Plants – II. Application to Harman Alkaloids of Genus Passiflora

Passiflora cincinnata

1 reference

High-Speed Extraction and HPLC Fingerprinting of Medicinal Plants – II. Application to Harman Alkaloids of Genus Passiflora

Passiflora citrina

1 reference

High-Speed Extraction and HPLC Fingerprinting of Medicinal Plants – II. Application to Harman Alkaloids of Genus Passiflora

Passiflora cuneata

1 reference

High-Speed Extraction and HPLC Fingerprinting of Medicinal Plants – II. Application to Harman Alkaloids of Genus Passiflora

Passiflora discophora

1 reference

High-Speed Extraction and HPLC Fingerprinting of Medicinal Plants – II. Application to Harman Alkaloids of Genus Passiflora

Passiflora edulis

2 references

High-Speed Extraction and HPLC Fingerprinting of Medicinal Plants – II. Application to Harman Alkaloids of Genus Passiflora

Pharmacochemical investigations on raw materials genus passiflora. 3. Phytochemical investigations on raw materials of passiflora edulis forma flavicarpa (author's transl)

Passiflora filipes

1 reference

High-Speed Extraction and HPLC Fingerprinting of Medicinal Plants – II. Application to Harman Alkaloids of Genus Passiflora

Passiflora foetida

1 reference

High-Speed Extraction and HPLC Fingerprinting of Medicinal Plants – II. Application to Harman Alkaloids of Genus Passiflora

Passiflora guatemalensis

1 reference

High-Speed Extraction and HPLC Fingerprinting of Medicinal Plants – II. Application to Harman Alkaloids of Genus Passiflora

Passiflora juliana

1 reference

High-Speed Extraction and HPLC Fingerprinting of Medicinal Plants – II. Application to Harman Alkaloids of Genus Passiflora

Passiflora laurifolia

1 reference

High-Speed Extraction and HPLC Fingerprinting of Medicinal Plants – II. Application to Harman Alkaloids of Genus Passiflora

Passiflora lobata

1 reference

High-Speed Extraction and HPLC Fingerprinting of Medicinal Plants – II. Application to Harman Alkaloids of Genus Passiflora

Passiflora lutea

1 reference

High-Speed Extraction and HPLC Fingerprinting of Medicinal Plants – II. Application to Harman Alkaloids of Genus Passiflora

Passiflora macrophylla

1 reference

High-Speed Extraction and HPLC Fingerprinting of Medicinal Plants – II. Application to Harman Alkaloids of Genus Passiflora

Passiflora maliformis

1 reference

High-Speed Extraction and HPLC Fingerprinting of Medicinal Plants – II. Application to Harman Alkaloids of Genus Passiflora

Passiflora manicata

1 reference

High-Speed Extraction and HPLC Fingerprinting of Medicinal Plants – II. Application to Harman Alkaloids of Genus Passiflora

Passiflora multiflora

1 reference

High-Speed Extraction and HPLC Fingerprinting of Medicinal Plants – II. Application to Harman Alkaloids of Genus Passiflora

Passiflora perfoliata

1 reference

High-Speed Extraction and HPLC Fingerprinting of Medicinal Plants – II. Application to Harman Alkaloids of Genus Passiflora

Passiflora phoenicia

1 reference

High-Speed Extraction and HPLC Fingerprinting of Medicinal Plants – II. Application to Harman Alkaloids of Genus Passiflora

Passiflora racemosa

1 reference

High-Speed Extraction and HPLC Fingerprinting of Medicinal Plants – II. Application to Harman Alkaloids of Genus Passiflora

Passiflora rubra

1 reference

High-Speed Extraction and HPLC Fingerprinting of Medicinal Plants – II. Application to Harman Alkaloids of Genus Passiflora

Passiflora sanguinolenta

1 reference

High-Speed Extraction and HPLC Fingerprinting of Medicinal Plants – II. Application to Harman Alkaloids of Genus Passiflora

Passiflora serratifolia

1 reference

High-Speed Extraction and HPLC Fingerprinting of Medicinal Plants – II. Application to Harman Alkaloids of Genus Passiflora

Passiflora sexflora

1 reference

High-Speed Extraction and HPLC Fingerprinting of Medicinal Plants – II. Application to Harman Alkaloids of Genus Passiflora

Passiflora subpeltata

1 reference

High-Speed Extraction and HPLC Fingerprinting of Medicinal Plants – II. Application to Harman Alkaloids of Genus Passiflora

Passiflora tenuifila

1 reference

High-Speed Extraction and HPLC Fingerprinting of Medicinal Plants – II. Application to Harman Alkaloids of Genus Passiflora

Passiflora tuberosa

1 reference

High-Speed Extraction and HPLC Fingerprinting of Medicinal Plants – II. Application to Harman Alkaloids of Genus Passiflora

Passiflora xiikzodz

1 reference

High-Speed Extraction and HPLC Fingerprinting of Medicinal Plants – II. Application to Harman Alkaloids of Genus Passiflora

Thalictrum foetidum

1 reference

Alkaloids of Thalictrum foetidum

Symplocos setchuensis

1 reference

Anti-AIDS agents. 46. Anti-HIV activity of harman, an anti-HIV principle from Symplocos setchuensis, and its derivatives

Carex brevicollis

1 reference

1,4-Substituted b-Carbolines from Carex brevicollis DC

Passiflora amethystina

1 reference

High-Speed Extraction and HPLC Fingerprinting of Medicinal Plants – II. Application to Harman Alkaloids of Genus Passiflora

Passiflora ampullacea

1 reference

High-Speed Extraction and HPLC Fingerprinting of Medicinal Plants – II. Application to Harman Alkaloids of Genus Passiflora

Festuca ovina

1 reference

Paper chromatography of alkaloids of tall fescue hay

Symplocos theifolia

1 reference

Anti-AIDS agents. 46. Anti-HIV activity of harman, an anti-HIV principle from Symplocos setchuensis, and its derivatives

Passiflora princeps

1 reference

High-Speed Extraction and HPLC Fingerprinting of Medicinal Plants – II. Application to Harman Alkaloids of Genus Passiflora

Erigeron canadensis

1 reference

Sphingolipids from Conyza canadensis

Grewia damine

1 reference

Investigation of Grewia bicolor Juss

subject has role

hallucinogen

1 reference

Medical Subject Headings

MeSH descriptor ID

D006247

monoamine oxidase inhibitor

15 March 2018

1 reference

InChI=1S/C13H12N2O/c1-8-13-11(5-6-14-8)10-4-3-9(16-2)7-12(10)15-13/h3-7,15H,1-2H3

Medical Subject Headings

15 March 2018

0 references

0 references

Harmine

0 references

Identifiers

InChI

1 reference

HARMINE (English)

19 November 2016

2 references

HARMINE (English)

19 November 2016

ChEBI release 2020-09-01

CAS Registry Number

442-51-3

2 references

Global Substance Registration System

harmine (English)

19 November 2016

https://commonchemistry.cas.org/detail?cas_rn=442-51-3

10 April 2021

1 reference

Harmine (English)

19 November 2016

1 reference

HARMINE (English)

19 November 2016

Reaxys registry number

178813

1 reference

harmine (English)

19 October 2016

mapping relation type

2 references

HARMINE (English)

19 November 2016

International Chemical Identifier

InChI

InChI=1S/C13H12N2O/c1-8-13-11(5-6-14-8)10-4-3-9(16-2)7-12(10)15-13/h3-7,15H,1-2H3

1 reference

HARMINE (English)

19 November 2016

2 references

inferred from InChIKey

MSBNK-Washington_State_Univ-BML01053

1 reference

MassBank accession ID

MSBNK-Fiocruz-FIO00120

0 references

MSBNK-Fiocruz-FIO00121

0 references

MSBNK-Fiocruz-FIO00122

0 references

MSBNK-Fiocruz-FIO00123

0 references

MSBNK-Fiocruz-FIO00124

0 references

MSBNK-Fiocruz-FIO00125

0 references

MSBNK-Fiocruz-FIO00126

0 references

MSBNK-Fiocruz-FIO00127

0 references

MSBNK-Fiocruz-FIO00128

0 references

MSBNK-Fiocruz-FIO00129

0 references

MSBNK-NaToxAq-NA000092

0 references

MSBNK-NaToxAq-NA000093

0 references

MSBNK-NaToxAq-NA000094

0 references

MSBNK-NaToxAq-NA000095

0 references

MSBNK-NaToxAq-NA000096

0 references

MSBNK-NaToxAq-NA000097

0 references

MSBNK-NaToxAq-NA000098

0 references

MSBNK-NaToxAq-NA000099

0 references

MSBNK-NaToxAq-NA000100

0 references

MSBNK-NaToxAq-NA000101

0 references

MSBNK-NaToxAq-NA000102

0 references

MSBNK-NaToxAq-NA000103

0 references

MSBNK-NaToxAq-NA000104

0 references

MSBNK-NaToxAq-NA000105

0 references

MSBNK-NaToxAq-NA000106

0 references

MSBNK-NaToxAq-NA000107

0 references

MSBNK-NaToxAq-NA000108

0 references

MSBNK-NaToxAq-NA000109

0 references

MSBNK-NaToxAq-NA000110

0 references

MSBNK-NaToxAq-NA000111

0 references

MSBNK-NaToxAq-NA000112

0 references

MSBNK-NaToxAq-NA000113

0 references

MSBNK-NaToxAq-NA000114

0 references

MSBNK-NaToxAq-NA000115

0 references

MSBNK-NaToxAq-NA000116

0 references

MSBNK-NaToxAq-NA000117

0 references

MSBNK-NaToxAq-NA000118

0 references

MSBNK-NaToxAq-NA000119

0 references

MSBNK-NaToxAq-NA000120

0 references

MSBNK-NaToxAq-NA000121

0 references

0 references

MSBNK-Washington_State_Univ-BML01056

0 references

MSBNK-Washington_State_Univ-BML01059

0 references

MSBNK-Washington_State_Univ-BML01062

0 references

MSBNK-Washington_State_Univ-BML01065

0 references

MSBNK-Washington_State_Univ-BML01068

0 references

MSBNK-Washington_State_Univ-BML81365

0 references

MSBNK-Washington_State_Univ-BML81366

0 references

MSBNK-Washington_State_Univ-BML81367

0 references

MSBNK-Washington_State_Univ-BML81368

0 references

SPLASH

splash10-03di-0195000000-4eb0eb565ba056865aa6

0 references

splash10-006t-0920000000-e68ee06c7ad898d448b0

0 references

splash10-00di-0950000000-996c89900776affe7b42

0 references

splash10-01b9-0950000000-8b5053cf47cac449fab7

0 references

splash10-03di-0195000000-fa0446e989509658da3d

0 references

splash10-0002-0910000000-4a6e6c341c4868149774

0 references

splash10-0002-0950000000-8d47230f745bacac3927

0 references

splash10-00kb-0950000000-16e41b0926f6f19e8e38

0 references

splash10-00kb-0950000000-8ad2d2db9ac2e4e33f2a

0 references

splash10-03di-0195000000-c155ccc223856b24d591

0 references

splash10-01ot-0950000000-012b0b00f2690f9f975d

0 references

splash10-00xr-0950000000-87c0ba2a9de84a712604

0 references

splash10-03dj-0980000000-f76e1f1ebc0a34cf9e19

0 references

splash10-0002-0950000000-10a7486ab11a55848f36

0 references

splash10-014j-0950000000-f96154ced990a53da1ed

0 references

splash10-03di-0095000000-9fe1bfdc579f703d2579

0 references

splash10-03di-0095000000-7a79ffb62da10112405f

0 references

splash10-03di-0095000000-2776c72395657337a6a7

0 references

splash10-00di-0910000000-c3bf098f88a09ca6c88a

0 references

splash10-00di-0920000000-b2bbb79b7783c3ddbfcb

0 references

NMRShiftDB structure ID

10018937

1 reference

DSSTox substance ID

DTXSID30196066

2 references

Mapping file of InChIStrings, InChIKeys and DTXSIDs for the EPA CompTox Dashboard

DSSTOX compound identifier

0 references

1 reference

Global Substance Registration System

harmine (English)

ECHA Substance Infocard ID

19 November 2016

100.006.485

1 reference

ECHA Substance Infocard database

ECHA Substance Infocard ID

27 December 2018

Harmine (English)

CAS no.: 442-51-3 (English)

Guide to Pharmacology Ligand ID

9352

1 reference

IUPHAR/BPS Guide to PHARMACOLOGY

5 February 2021

Harmine

0 references

MeSH tree code

D03.132.436.384.500

0 references

D03.633.100.473.402.222.500

0 references

D03.633.100.496.500.500.384.500

0 references

D03.633.300.154.344

0 references

DrugBank ID

DB07919

1 reference

Human Metabolome Database ID

HMDB0030311

2 references

based on heuristic

inferred from InChIKey

3 references

harmine (English)

19 October 2016

inferred from InChIKey

2 references

Global Substance Registration System

harmine (English)

19 November 2016

imported from Wikimedia project

0 references

1 reference

0 references

0 references

Encyclopædia Britannica Online ID

science/harmine

subject named as

harmine

0 references

1 reference

28 October 2013

Microsoft Academic ID

2781450507

0 references

Open Library subject ID

0 references

1 reference

26 January 2022

https://docs.openalex.org/download-snapshot/snapshot-data-format

1 reference

3ANR (English)

19 October 2016

1 reference

2Z5X (English)

19 October 2016

1 reference

inferred by common MeSH mappings on source and on Wikidata

2Z5Y (English)

19 October 2016

1 reference

UMLS 2023